Literature DB >> 15698538

Major impact of hormonal therapy in localized prostate cancer--death can already be an exception.

Fernand Labrie1, Leonello Cusan, José Gomez, Van Luu-The, Bernard Candas, Alain Bélanger, Claude Labrie.   

Abstract

For about 50 years, androgen blockade in prostate cancer has been limited to monotherapy (surgical castration) or high doses of estrogens in patients with advanced disease and bone metastases. The discovery of medical castration with LHRH agonists has led to fundamental changes in the endocrine therapy of prostate cancer. In 1979, the first prostate cancer patient treated with an LHRH agonist received such treatment at the Laval University Medical Center. A long series of studies have clearly demonstrated that medical castration with an LHRH agonist has inhibitory effects on prostate cancer equivalent to those of surgical castration. The much higher acceptability of LHRH agonists has been essential to permit a series of studies in localized disease. Based upon the finding that the testicles and adrenals contribute approximately equal amounts of androgens in the human prostate, the combination of medical (LHRH agonist) or surgical castration associated with a pure antiandrogen (flutamide, nilutamide or bicalutamide) has led to the first demonstration of a prolongation of life in prostate cancer, namely a 10-20% decreased risk of death according to the various metaanalyses of all the studies performed in advanced disease. In analogy with the other types of advanced cancers, the success of combined androgen blockade in metastatic disease is limited by the development of resistance to treatment. To avoid the problem of resistance to treatment while taking advantage of the relative ease of diagnosis of prostate cancer at an "early" stage, the much higher acceptability of LHRH agonists has permitted a series of studies which have demonstrated a major reduction in deaths from prostate cancer ranging from 31% to 87% at 5 years of follow-up in patients with localized or locally advanced prostate cancer. Most importantly, recent data show that the addition of a pure antiandrogen to an LHRH agonist in order to block the androgens made locally in the prostate leads to a 90% long-term control or probable cure of prostate cancer.

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Year:  2004        PMID: 15698538     DOI: 10.1016/j.jsbmb.2004.10.011

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  4 in total

1.  Development, validation and application of a stable isotope dilution liquid chromatography electrospray ionization/selected reaction monitoring/mass spectrometry (SID-LC/ESI/SRM/MS) method for quantification of keto-androgens in human serum.

Authors:  Daniel Tamae; Michael Byrns; Brett Marck; Elahe A Mostaghel; Peter S Nelson; Paul Lange; Daniel Lin; Mary-Ellen Taplin; Steven Balk; William Ellis; Larry True; Robert Vessella; Bruce Montgomery; Ian A Blair; Trevor M Penning
Journal:  J Steroid Biochem Mol Biol       Date:  2013-07-10       Impact factor: 4.292

Review 2.  The basic biochemistry and molecular events of hormone therapy.

Authors:  Elahe A Mostaghel; Robert B Montgomery; Daniel W Lin
Journal:  Curr Urol Rep       Date:  2007-05       Impact factor: 3.092

Review 3.  Clinical relevance of androgen receptor alterations in prostate cancer.

Authors:  Emma Jernberg; Anders Bergh; Pernilla Wikström
Journal:  Endocr Connect       Date:  2017-11       Impact factor: 3.335

Review 4.  Androgen Receptor-CaMKK2 Axis in Prostate Cancer and Bone Microenvironment.

Authors:  Ushashi C Dadwal; Eric S Chang; Uma Sankar
Journal:  Front Endocrinol (Lausanne)       Date:  2018-06-18       Impact factor: 5.555

  4 in total

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